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This work is licensed under a Creative Commons Attribution 4.0 International License.
SiO2:MgMnO3: An Efficient Heterogeneous Catalyst for One Pot Synthesis of 1H-Pyrazolo[1,2-b]phthalazine-5,10-dione Derivatives
Corresponding Author(s) : S.S. Sagar
Asian Journal of Chemistry,
Vol. 32 No. 10 (2020): Vol 32 Issue 10
Abstract
The present study deals with hydrothermal synthesis of SiO2 composite MgMnO3 catalyst. The obtained polycrystalline product was analyzed by using physical investigative techniques including XRD, SEM, EDAX, TEM, SAED and BET surface area. The product corresponded to average particle size of 100 nm by TEM images. The BET surface area was found 234.38 cm2/g for SiO2 composite MgMnO3 catalyst which indicates a good catalytic property. The synthesized catalyst was applied for the synthesis of 1H-pyrazolo[1,2-b]-phthalazine-5,10-dione in presence of ethanol as a solvent at 80 ºC. The current procedure and catalyst offers the gains of clean reaction, short reaction time, high yield, easy purification and financial availability of the catalyst.
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References
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N.K. Terrett, A.S. Bell, D. Brown and P. Ellis, Bioorg. Med. Chem. Lett., 6, 1819 (1996); https://doi.org/10.1016/0960-894X(96)00323-X
S.K. Singh, P.G. Reddy, K.S. Rao, B.B. Lohray, P. Misra, S.A. Rajjak, Y.K. Rao and A. Venkateswarlu, Bioorg. Med. Chem. Lett., 14, 499 (2004); https://doi.org/10.1016/j.bmcl.2003.10.027
J. Li, Y.F. Zhao, X.Y. Yuan, J.X. Xu and P. Gong, Molecules, 11, 574 (2006); https://doi.org/10.3390/11070574
S.S. El-Sakka, A.H. Soliman and A.M. Imam, Afinidad, 66, 167 (2009).
C.K. Ryu, R.E. Park, M.-Y. Ma and J.-H. Nho, Bioorg. Med. Chem. Lett., 17, 2577 (2007); https://doi.org/10.1016/j.bmcl.2007.02.003
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K. Hemming, Annu. Rep. Prog. Chem. B, 107, 118 (2011); https://doi.org/10.1039/c1oc90016a
A. Dömling and I. Ugi, Angew. Chem. Int. Ed. Engl., 39, 3168 (2000); https://doi.org/10.1002/1521-3773(20000915)39:18<3168::AIDANIE3168>3.0.CO;2-U
T.J. Müller, Beilstein J. Org. Chem., 7, 960 (2011); https://doi.org/10.3762/bjoc.7.107
R. Ghahremanzadeh, G.I. Shakibaei and A. Bazgir, Synlett, 8, 1129 (2008); https://doi.org/10.1055/s-2008-1072716
M.R. Nabid, S.J.T. Rezaei, R. Ghahremanzadeh and A. Bazgir, Ultrason. Sonochem., 17, 159 (2010); https://doi.org/10.1016/j.ultsonch.2009.06.012
D.S. Raghuvanshi and K.N. Singh, Tetrahedron Lett., 52, 5702 (2011); https://doi.org/10.1016/j.tetlet.2011.08.111
H.R. Shaterian and M. Mohammadnia, J. Mol. Liq., 173, 55 (2012); https://doi.org/10.1016/j.molliq.2012.06.007
G. Karthikeyan and A. Pandurangan, J. Mol. Catal. Chem., 361-362, 58 (2012); https://doi.org/10.1016/j.molcata.2012.05.003
S.H. Song, J. Zhong, Y.H. He and Z. Guan, Tetrahedron Lett., 53, 7075 (2012); https://doi.org/10.1016/j.tetlet.2012.10.063
M.V. Reddy and Y.T. Jeong, Tetrahedron Lett., 54, 3546 (2013); https://doi.org/10.1016/j.tetlet.2013.04.109
R. Imbihl, M.P. Cox, G. Ertl, H. Müller and W. Brenig, J. Chem. Phys., 83, 1578 (1985); https://doi.org/10.1063/1.449834
K. Kuzushita, S. Morimota and S. Nasu, Physica B, 329-333, 736 (2003); https://doi.org/10.1016/S0921-4526(02)02478-X